Survivin-directed RNA interference-compositions and methods
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Analysis of Survivin Protein Expression in Pediatric Rhabdomyosarcoma Tissue Samples
[0066] Expression of survivin-protein was evaluated in 63 primary human RMS tumors that included 31 embryonal rhabdomyosarcoma (ERMS) and 32 alveolar rhabdomyosarcoma (ARMS) tumors by immunohistochemical staining with a polyclonal antibody against survivin (FL-142, Santa Cruz).
[0067] Over 80% of the tumors analyzed for survivin protein expression (54 / 63 tumors) had a mean survivin staining score greater than or equal to 3, indicating that at least 10 to 50% of tumor cells expressed survivin
example 2
Analysis of Survivin RNA Expression in Rhabdomyosarcoma Cell Lines
[0068] Survivin RNA expression was examined in four representative RMS cell lines by quantitative PCR. Three cell lines were alveolar in origin (CW9019, RH28 and RH30) and one was embryonal (RD2).
[0069] Total RNA was isolated from 106 cells for each cell line using the Trizol® method (Invitrogen). cDNA was obtained in a random priming reaction using Omniscript reverse transcriptase (Qiagen). Primers to detect human survivin message and splice variants were designed according to the Applied Biosystem's Primer Express™ software, to quantify relative cDNA expression levels (Survivin: Forward 5′ GTG AAT TTT TGA AAC TGG ACA GAG AAA (Seq ID NO: 13); Reverse 5′ CAC TTT CTT CGC AGT TTC CTC AA (Seq ID NO: 14); Probe 5′ FAM AGC CAA GAA CAA AAT TGC AAA GGA AAC CA (Seq ID NO: 15); Survivin-2B: Forward 5′ GCA CGG TGG CTT ACG CCT G (Seq ID NO: 16); Reverse 5′ ACC GGA CGA ATG CTT TTT ATG TTC C (Seq ID NO: 17); Probe 5′ FAM ATA CCA...
example 3
Methods of Monitoring Survivin Inhibition
[0071] A cocktail of 3 DNA plasmids encoding survivin-specific shRNAs comprising SEQ ID NO: 1, SEQ ID NO: 2 and SEQ ID NO 3, that targeted different regions of the human survivin gene was used to eliminate survivin m-RNA in target cells (FIG. 2). The following oligonucleotides encoding the shRNAs were designed using software provided by OligoEngine company. Oligonucleotides 4 and 5 were used for the sh-RNA comprising SEQ ID NO: 1, oligonucleotides 6 and 7 were used for the sh-RNA comprising SEQ ID NO: 2 and oligonucleotides 8 and 9 were used for the sh-RNA comprising SEQ ID NO: 3. Each oligonucleotide pair was annealed, phosphorylated and cloned into Bgl II and Hind III restriction sited of pSUPER vector from OligoEngine company.
[0072] For transient transfections, plasmid DNA was transfected into proliferating CW9019 or RH30 cells using effectene transfection reagent (Qiagen) at a ratio of 1:30 (DNA:Effectene). The reporter plasmid pHcRed (...
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